TY - JOUR
T1 - Neuroimaging in infants with congenital cytomegalovirus infection and its correlation with outcome
T2 - emphasis on white matter abnormalities
AU - Alarcón, Ana
AU - de Vries, Linda S
AU - Parodi, Alessandro
AU - Arnáez, Juan
AU - Cabañas, Fernando
AU - Steggerda, Sylke J
AU - Rebollo, Mónica
AU - Ramenghi, Luca
AU - Dorronsoro, Izaskun
AU - López-Azorín, Manuela
AU - Schneider, Juliane
AU - Noguera-Julian, Antoni
AU - Ríos-Barnés, María
AU - Recio, Manuel
AU - Bickle-Graz, Myriam
AU - Martínez-Biarge, Miriam
AU - Fortuny, Clàudia
AU - García-Alix, Alfredo
AU - Truttmann, Anita C
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2024.
PY - 2024/2/19
Y1 - 2024/2/19
N2 - Objective: To evaluate the association between neuroimaging and outcome in infants with congenital cytomegalovirus (cCMV), focusing on qualitative MRI and quantitative diffusion-weighted imaging of white matter abnormalities (WMAs). Methods: Multicentre retrospective cohort study of 160 infants with cCMV (103 symptomatic). A four-grade neuroimaging scoring system was applied to cranial ultrasonography and MRI acquired at ≤3 months. WMAs were categorised as multifocal or diffuse. Temporal-pole WMAs (TPWMAs) consisted of swollen or cystic appearance. Apparent diffusion coefficient (ADC) values were obtained from frontal, parieto-occipital and temporal white matter regions. Available follow-up MRI at ≥6 months (N=14) was additionally reviewed. Neurodevelopmental assessment included motor function, cognition, behaviour, hearing, vision and epilepsy. Adverse outcome was defined as death or moderate/severe disability. Results: Neuroimaging scoring was associated with outcome (p<0.001, area under the curve 0.89±0.03). Isolated WMAs (IWMAs) were present in 61 infants, and WMAs associated with other lesions in 30. Although TPWMAs and diffuse pattern often coexisted in infants with IWMAs (p<0.001), only TPWMAs were associated with adverse outcomes (OR 7.8; 95% CI 1.4 to 42.8), including severe hearing loss in 20% and hearing loss combined with other moderate/severe disabilities in 15%. Increased ADC values were associated with higher neuroimaging scores, WMAs based on visual assessment and IWMAs with TPWMAs. ADC values were not associated with outcome in infants with IWMAs. Findings suggestive of progression of WMAs on follow-up MRI included gliosis and malacia. Conclusions: Categorisation of neuroimaging severity correlates with outcome in cCMV. In infants with IWMAs, TPWMAs provide a guide to prognosis.
AB - Objective: To evaluate the association between neuroimaging and outcome in infants with congenital cytomegalovirus (cCMV), focusing on qualitative MRI and quantitative diffusion-weighted imaging of white matter abnormalities (WMAs). Methods: Multicentre retrospective cohort study of 160 infants with cCMV (103 symptomatic). A four-grade neuroimaging scoring system was applied to cranial ultrasonography and MRI acquired at ≤3 months. WMAs were categorised as multifocal or diffuse. Temporal-pole WMAs (TPWMAs) consisted of swollen or cystic appearance. Apparent diffusion coefficient (ADC) values were obtained from frontal, parieto-occipital and temporal white matter regions. Available follow-up MRI at ≥6 months (N=14) was additionally reviewed. Neurodevelopmental assessment included motor function, cognition, behaviour, hearing, vision and epilepsy. Adverse outcome was defined as death or moderate/severe disability. Results: Neuroimaging scoring was associated with outcome (p<0.001, area under the curve 0.89±0.03). Isolated WMAs (IWMAs) were present in 61 infants, and WMAs associated with other lesions in 30. Although TPWMAs and diffuse pattern often coexisted in infants with IWMAs (p<0.001), only TPWMAs were associated with adverse outcomes (OR 7.8; 95% CI 1.4 to 42.8), including severe hearing loss in 20% and hearing loss combined with other moderate/severe disabilities in 15%. Increased ADC values were associated with higher neuroimaging scores, WMAs based on visual assessment and IWMAs with TPWMAs. ADC values were not associated with outcome in infants with IWMAs. Findings suggestive of progression of WMAs on follow-up MRI included gliosis and malacia. Conclusions: Categorisation of neuroimaging severity correlates with outcome in cCMV. In infants with IWMAs, TPWMAs provide a guide to prognosis.
KW - Deafness
KW - Infectious Disease Medicine
KW - Magnetic Resonance Imaging
KW - Neonatology
KW - Neurology
UR - http://www.scopus.com/inward/record.url?scp=85173061315&partnerID=8YFLogxK
U2 - 10.1136/archdischild-2023-325790
DO - 10.1136/archdischild-2023-325790
M3 - Article
C2 - 37739774
SN - 1359-2998
VL - 109
SP - 151
EP - 158
JO - Archives of Disease in Childhood Fetal and Neonatal Edition
JF - Archives of Disease in Childhood Fetal and Neonatal Edition
IS - 2
M1 - archdischild-2023-325790
ER -